Causative TP63 mutations have been identified in five distinct human developmental disorders that are characterized by various degrees of limb abnormalities, ectodermal dysplasia, and facial clefts. The distribution of mutations over the various p63 protein domains and the structural and functional implications of these mutations establish a clear genotype-phenotype correlation
p63 mutations have been associated with EEC syndrome (ectrodactyly, ectodermal dysplasia, and cleft ...
p63 is the most recently discovered but most ancient member of the p53 family. In marked contrast to...
Heterozygous mutations in the p63 gene underlie a group of at least seven allelic syndromes, includi...
Causative TP63 mutations have been identified in five distinct human developmental disorders that ar...
Causative TP63 mutations have been identified in five distinct human developmental disorders that ar...
Mutations in the transcription factor gene p63 are causative for human developmental syndromes chara...
Contains fulltext : 52497.pdf (publisher's version ) (Open Access)Heterozygous mut...
The P63 gene is a recently discovered member of the p53 family. While P53 is ubiquitously expressed,...
Heterozygous mutations in the transcription factor gene p63 cause at least six different syndromes w...
Item does not contain fulltextSeveral autosomal dominantly inherited human syndromes have recently b...
Heterozygous mutations in TP63 cause a wide spectrum of autosomal dominant developmental disorders v...
TP63-related disorders comprise a group of six overlapping autosomal dominant (AD) syndromes caused ...
The p63 gene is a transcription factor and a member of the p53 family. Heterozygote mutation of the ...
Individuals with Tumor Protein P63 (TP63)-related disorders are known to present with a range of phe...
p63 mutations have been associated with EEC syndrome (ectrodactyly, ectodermal dysplasia, and cleft ...
p63 mutations have been associated with EEC syndrome (ectrodactyly, ectodermal dysplasia, and cleft ...
p63 is the most recently discovered but most ancient member of the p53 family. In marked contrast to...
Heterozygous mutations in the p63 gene underlie a group of at least seven allelic syndromes, includi...
Causative TP63 mutations have been identified in five distinct human developmental disorders that ar...
Causative TP63 mutations have been identified in five distinct human developmental disorders that ar...
Mutations in the transcription factor gene p63 are causative for human developmental syndromes chara...
Contains fulltext : 52497.pdf (publisher's version ) (Open Access)Heterozygous mut...
The P63 gene is a recently discovered member of the p53 family. While P53 is ubiquitously expressed,...
Heterozygous mutations in the transcription factor gene p63 cause at least six different syndromes w...
Item does not contain fulltextSeveral autosomal dominantly inherited human syndromes have recently b...
Heterozygous mutations in TP63 cause a wide spectrum of autosomal dominant developmental disorders v...
TP63-related disorders comprise a group of six overlapping autosomal dominant (AD) syndromes caused ...
The p63 gene is a transcription factor and a member of the p53 family. Heterozygote mutation of the ...
Individuals with Tumor Protein P63 (TP63)-related disorders are known to present with a range of phe...
p63 mutations have been associated with EEC syndrome (ectrodactyly, ectodermal dysplasia, and cleft ...
p63 mutations have been associated with EEC syndrome (ectrodactyly, ectodermal dysplasia, and cleft ...
p63 is the most recently discovered but most ancient member of the p53 family. In marked contrast to...
Heterozygous mutations in the p63 gene underlie a group of at least seven allelic syndromes, includi...
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